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Characterizing Difficulty and Life Disruption During B-Acute Lymphoblastic Leukemia Therapy From the Perspective of
Kellee N Parker1, Sarah W Alexander2, Lisa M Jacola3
1Department of Pediatrics, University of Utah, Salt Lake City, Utah, USA.
Insights
Parents find childhood B-acute lymphoblastic leukemia (B-ALL) treatment difficult due to side effects like nausea and vomiting, and care aspects like hospital visits. Understanding these challenges is key to improving pediatric cancer care.
Area of Science:
- Pediatric Oncology
- Childhood Cancer Survivorship
- Patient-Reported Outcomes
Background:
- Childhood B-acute lymphoblastic leukemia (B-ALL) treatment is lengthy and toxic, despite high cure rates in developed settings.
- Understanding parental perspectives on treatment burdens is crucial for enhancing pediatric cancer care.
- Previous research has not fully captured the specific difficulties parents face during B-ALL treatment.
Purpose of the Study:
- To identify child side effects, chemotherapeutic agents, and care aspects parents perceive as most difficult or disruptive during B-ALL treatment.
- To explore variations in these perceptions based on child or parent characteristics.
- To inform future improvements in B-ALL treatment regimens and supportive care.
Main Methods:
- An online survey was administered to parents of children (aged 1-19 years) diagnosed with B-ALL.
- Participants were members of the Momcology pediatric cancer support and advocacy organization.
- Data were analyzed descriptively, with inferential statistics used to examine characteristic-based differences.
Main Results:
- Nausea/vomiting, decreased energy, and neuropathy were common difficult side effects during pre-maintenance therapy.
- Mood changes were the most difficult side effect during maintenance therapy.
- Oral corticosteroids, unplanned hospital visits, and compromised immunity were rated as the most difficult/disruptive aspects of care.
Conclusions:
- Treatment for childhood B-ALL imposes significant difficulties on children and their families.
- Parent-reported challenges highlight critical areas for optimizing treatment protocols and supportive care strategies.
- Addressing treatment-related toxicities and logistical burdens is essential for improving the quality of life for children with B-ALL.
Purpose:
Children with B-acute lymphoblastic leukemia (B-ALL) treated in resource-intensive settings have a high likelihood of cure, but therapy is long, burdensome, and associated with substantial toxicities. Understanding parents' perceptions of the most disruptive and difficult aspects of B-ALL treatment is critical to future improvements in care. We aimed to understand which child side effects, chemotherapeutic agents, and aspects of leukemia care are rated difficult or disruptive by parents, and variations based on parent or child characteristics.
Methods:
Parents of children (1-19 years) currently or previously treated for B-ALL who are members of the Momcology pediatric cancer support and advocacy organization were invited to complete an online survey on difficult and disruptive aspects associated with their child's diagnosis. Data were analyzed descriptively, and inferential statistical tests evaluated characteristic-based differences.
Results:
Parents of 442 children completed the survey. Nausea/vomiting was the most commonly reported difficult side effect during pre-maintenance therapy (55.4%), followed by decreased energy (41.4%) and neuropathy (40.7%). Mood changes were the most difficult side effect during maintenance therapy (29.3%). The extent of difficulty associated with each side effect reported was high. Most parents (79.6%) rated oral corticosteroids as the most difficult chemotherapeutic agent. The components of care most difficult and disruptive were unplanned hospital visits (79.9%) and compromised immunity (76.9%). Parent-rated difficulties significantly varied by child age at diagnosis.
Conclusions:
Parents of children with B-ALL report substantial child and family difficulties that are directly attributable to leukemia treatment. These findings should inform areas of investigation for optimizing treatment regimens and supportive care.
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